Variant report

Variant	rs183897402
Chromosome Location	chr11:64911731-64911732
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 2 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv526181	chr11:64638041-65257329	Flanking Active TSS Enhancers Strong transcription Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1539 gene(s)	inside rSNPs	diseases
2	nsv972038	chr11:64911552-64913423	Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:64903600-64911800	Weak transcription	Spleen	Spleen
2	chr11:64903600-64917400	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr11:64904200-64913400	Weak transcription	Primary B cells from cord blood	blood
4	chr11:64910200-64912200	Weak transcription	Liver	Liver
5	chr11:64910200-64913000	Weak transcription	Primary B cells from peripheral blood	blood
6	chr11:64910200-64913800	Weak transcription	HepG2	liver
7	chr11:64911200-64911800	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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